The association between NDUFS6 (NADH:Ubiquinone Oxidoreductase Subunit S6) and Mitochondrial Complex I Deficiency, Nuclear Type 1 is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording a causative germline mutation.
Sources2
Clinical variants25
Symptoms96
Compounds0
Trials0
Publications3
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.